Department of Biological Sciences, Faculty of Biosciences and Bioengineering, Universiti Teknologi Malaysia, Johor, Malaysia.
FEMS Microbiol Lett. 2011 May;318(2):108-14. doi: 10.1111/j.1574-6968.2011.02245.x. Epub 2011 Mar 8.
Genes involved in the 4-aminobenzenesulfonate (4-ABS) degradation pathway of Hydrogenophaga sp. PBC were identified using transposon mutagenesis. The screening of 10,000 mutants for incomplete 4-ABS biotransformation identified four mutants with single transposon insertion. Genes with insertions that impaired the ability to utilize 4-ABS for growth included (1) 4-sulfocatechol 1,2-dioxygenase β-subunit (pcaH2) and 3-sulfomuconate cycloisomerase involved in the modified β-ketoadipate pathway; (2) 4-aminobenzenesulfonate 3,4-dioxygenase component (sadA) involved in aromatic ring hydroxylation; and (3) transposase gene homolog with a putative cis-diol dehydrogenase gene located downstream. The pcaH2 mutant strain accumulated brown metabolite during growth on 4-ABS which was identified as 4-sulfocatechol through thin layer chromatography and HPLC analyses. Supplementation of wild-type sadA gene in trans restored the 4-ABS degradation ability of the sadA mutant, thus supporting the annotation of its disrupted gene.
利用转座子突变技术鉴定了氢噬菌属 PBC 中 4-氨基苯磺酸盐(4-ABS)降解途径相关的基因。对 10000 个不完全 4-ABS 生物转化突变体进行筛选,发现了 4 个带有单个转座子插入的突变体。插入导致丧失利用 4-ABS 进行生长能力的基因包括(1)参与修饰的β-酮己二酸途径的 4-磺基儿茶酚 1,2-双加氧酶β亚基(pcaH2)和 3-磺基戊二酸环异构酶;(2)参与芳香环羟化的 4-氨基苯磺酸盐 3,4-加双氧酶组分(sadA);和(3)位于下游的转座酶基因同源物和推定的顺式二醇脱氢酶基因。在 4-ABS 上生长时,pcaH2 突变株积累了棕色代谢物,通过薄层层析和 HPLC 分析鉴定为 4-磺基儿茶酚。野生型 sadA 基因的互补恢复了 sadA 突变体的 4-ABS 降解能力,因此支持其破坏基因的注释。